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Versatile enantiocontrolled synthesis of (+)-fostriecin
Authors:Esumi Tomoyuki  Okamoto Nanako  Hatakeyama Susumi
Affiliation:Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan. susumi@net.nagasaki-u.ac.jp
Abstract:Fostriecin, a potent protein phosphatase inhibitor and antitumor agent, has been enantioselectively synthesized in naturally occurring form via a versatile route, which also allows one to secure all possible stereoisomeres of the C1-C13 fragment including the C11 stereocenter and the geometry of the delta 12-double bond.
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